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Epigenetic and Transcriptional Regulations in Pancreatic Ductal Adenocarcinoma.
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Epigenetic and Transcriptional Regulations in Pancreatic Ductal Adenocarcinoma.
자료유형  
 학위논문
Control Number  
0017162711
International Standard Book Number  
9798384482406
Dewey Decimal Classification Number  
574
Main Entry-Personal Name  
Xu, Reno Jiaho.
Publication, Distribution, etc. (Imprint  
[S.l.] : University of California, Davis., 2024
Publication, Distribution, etc. (Imprint  
Ann Arbor : ProQuest Dissertations & Theses, 2024
Physical Description  
202 p.
General Note  
Source: Dissertations Abstracts International, Volume: 86-04, Section: B.
General Note  
Advisor: Hwang, Chang-il.
Dissertation Note  
Thesis (Ph.D.)--University of California, Davis, 2024.
Summary, Etc.  
요약Pancreatic ductal adenocarcinoma (PDA) presents a significant challenge in oncology due to its aggressive nature and limited treatment options. Despite advancements in understanding the genomic landscape of PDA initiation and progression, the mechanisms driving metastasis remain elusive. This doctoral thesis explores the critical role of epigenetic mechanisms, specifically focusing on transcriptional regulation, histone modification, and molecular crowding in PDA metastasis. Through a multidisciplinary approach, encompassing genomic analyses, functional studies, and biophysical investigations, the thesis sheds light on the intricate interplay between genetic and epigenetic factors driving PDA progression. Chapters elucidate the aberrant expression of the homeodomain transcription factor EN1 in PDA, its impact on downstream signaling pathways, and its promotion of PDA transformation and metastasis. Furthermore, the thesis uncovers the influence of nucleoplasmic macromolecular crowding, particularly highlighting the role of nesprin-3, in regulating nuclear dynamics and metastatic potential in PDA. By integrating genetic, epigenetic, and biophysical perspectives, this work not only advances our understanding of PDA pathogenesis but also paves the way for the development of targeted therapeutic interventions. Additionally, the thesis underscores the significance of pancreatic cancer organoid models in recapitulating disease progression, elucidating molecular dynamics, and guiding precision medicine approaches. Overall, this research underscores the importance of a comprehensive approach in deciphering the complexities of PDA and offers valuable insights for future therapeutic strategies aimed at improving patient outcomes.
Subject Added Entry-Topical Term  
Biology.
Subject Added Entry-Topical Term  
Cellular biology.
Subject Added Entry-Topical Term  
Oncology.
Subject Added Entry-Topical Term  
Molecular biology.
Subject Added Entry-Topical Term  
Biochemistry.
Index Term-Uncontrolled  
Pancreatic ductal adenocarcinoma
Index Term-Uncontrolled  
Molecular crowding
Index Term-Uncontrolled  
Transcriptional regulations
Index Term-Uncontrolled  
Epigenetic mechanisms
Index Term-Uncontrolled  
Pancreatic cancer metastasis
Added Entry-Corporate Name  
University of California, Davis Biochemistry Molecular Cellular and Developmental Biology
Host Item Entry  
Dissertations Abstracts International. 86-04B.
Electronic Location and Access  
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Control Number  
joongbu:654214
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